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1 n 70 (HSP70) IgG was isolated from plasma by immunoaffinity.
2 GFR protein (CD271, p75NTR) were isolated by immunoaffinity adsorption, and cultured as a monolayer f
3 m complex biological samples, without use of immunoaffinity agents.
4                                           By immunoaffinity and enzyme-linked immunosorbent assay tec
5                                        Using immunoaffinity and high-performance liquid chromatograph
6                                        After immunoaffinity and HPLC purification, MALDI/MS measured
7 f patients with pancreatic cancer, including immunoaffinity and label-free physical attribute-based c
8  combines the selectivity and sensitivity of immunoaffinity and mass spectrometric based techniques f
9     Using a variety of approaches, including immunoaffinity and mass spectrometry, we identified a pr
10 f >10 mg of monomeric hOR17-4 receptor after immunoaffinity and size exclusion chromatography, with e
11       Macrophage exosomes and MV isolated by immunoaffinity and sucrose cushion centrifugation were c
12                                     Using an immunoaffinity approach followed by multipoint validatio
13  (hSPC25) and human SPC24 (hSPC24), using an immunoaffinity approach.
14  from neutrophil lysates with an anti-ICAM-3 immunoaffinity assay.
15                                              Immunoaffinity assays are the workhorse for measuring in
16 observations demonstrate the utility of CD45 immunoaffinity-based approaches for producing highly pur
17 rochannel and also a technique for improving immunoaffinity-based circulating tumor cell (CTC) captur
18               In the work presented here, an immunoaffinity-based LC/MS/MS assay was developed and va
19                            The assay uses an immunoaffinity-based liquid chromatography-tandem mass s
20 that is a simple and reliable alternative to immunoaffinity-based methods.
21                         We report here a new immunoaffinity-based purification procedure for TLF2 and
22 c monoclonal antibodies and therefore, allow immunoaffinity-based purification.
23 as isolated through binding of either tag to immunoaffinity beads and then decorated with antibodies
24 use in surface plasmon resonance (SPR)-based immunoaffinity biosensors.
25  cow's milk allergy has been performed using immunoaffinity capillary electrophoresis (IACE) coupled
26          We utilized a novel microchip-based immunoaffinity capillary electrophoresis technology to m
27                                              Immunoaffinity capture and mass spectrometry revealed as
28 say that uses sequential protein and peptide immunoaffinity capture for protein target quantitation.
29                            We established an immunoaffinity capture LC-HRMS method to quantify the in
30 nd AhR knockdown H358 cells was validated by immunoaffinity capture stable isotope dilution ([(15)N(5
31                                    Following immunoaffinity chromatographic purification from rat liv
32 pressed in E. coli, and purified by a single immunoaffinity chromatographic step using a monoclonal a
33 sed, incorporating on-line, high-performance immunoaffinity chromatography (HPIAC).
34                                              Immunoaffinity chromatography (IAC) was used to isolate
35 V detection, after prior matrix isolation by immunoaffinity chromatography (IAC).
36 fied ISGylated proteins from human thymus by immunoaffinity chromatography and analyzed ISG15 conjuga
37 ctrometry (MS/MS) assay that utilizes online immunoaffinity chromatography and column switching was d
38 , we isolated apo(a)-containing particles by immunoaffinity chromatography and determined the concent
39 ted complexes containing PLTP from plasma by immunoaffinity chromatography and determined their compo
40                           We performed ATP7A immunoaffinity chromatography and identified 541 protein
41 he intervention measured by using sequential immunoaffinity chromatography and liquid chromatography-
42                       Using a combination of immunoaffinity chromatography and mass spectrometry, we
43 f serpin-6 and PAP-3 in induced hemolymph by immunoaffinity chromatography and mass spectrometry.
44                                      We used immunoaffinity chromatography and mass spectroscopy to i
45 300 gel filtration chromatography, anti-FLAG immunoaffinity chromatography and SDS/PAGE permitted pur
46                                        Using immunoaffinity chromatography and tandem mass spectromet
47 zed receptor was easily purified by one-step immunoaffinity chromatography and the purified receptor
48      In this study, we applied an integrated immunoaffinity chromatography and top-down MS approach t
49  as separated by anti-apoC-III and anti-apoE immunoaffinity chromatography and ultracentrifugation in
50 d several mutants, from transfected cells by immunoaffinity chromatography and visualized individual
51 say methods were developed for detection and immunoaffinity chromatography capture was developed for
52      PAP-serpin-3 complexes were isolated by immunoaffinity chromatography from hemolymph activated b
53 C heterocomplex was isolated and purified by immunoaffinity chromatography from insect cells co-expre
54 is mAb, isolation of the troponin complex by immunoaffinity chromatography from muscle homogenate and
55 hain, cross-linked peptides were isolated by immunoaffinity chromatography from proteolytic digests o
56 on, Inc., Sunnyvale, Calif.) was purified by immunoaffinity chromatography from supernatant fluids of
57 from rod outer segments of bovine retinae by immunoaffinity chromatography in octyl glucoside was rec
58                           Anion exchange and immunoaffinity chromatography indicated that the (1-->4)
59                                              Immunoaffinity chromatography is one of the most powerfu
60 s of the protein to facilitate separation by immunoaffinity chromatography of overproduced mutant enz
61 e (EEF) tripepetide to allow purification by immunoaffinity chromatography on an immobilized monoclon
62 d from the soluble fraction by a single-step immunoaffinity chromatography procedure.
63                          Finally, we discuss immunoaffinity chromatography results that suggest the e
64 extracts by a combination of traditional and immunoaffinity chromatography steps and found that the p
65 from HeLa cell extracts using two successive immunoaffinity chromatography steps.
66 olution mass spectrometry (MS) combined with immunoaffinity chromatography to determine quantitativel
67 nt signaling, we used cell fractionation and immunoaffinity chromatography to examine the physical en
68                  In this study, we have used immunoaffinity chromatography to identify proteins that
69 o identify new vaccine targets, we have used immunoaffinity chromatography to isolate class I HLA-A*0
70  pump-generated flow to deliver reagents and immunoaffinity chromatography to isolate the antigen fro
71                                      We used immunoaffinity chromatography to isolate the naturally p
72 nds the powerful technique of gentle-release immunoaffinity chromatography to many expressed proteins
73                                      We used immunoaffinity chromatography to measure the apoA-I conc
74 control children (n = 54), we used recycling immunoaffinity chromatography to measure the neuropeptid
75 f conventional chromatography and anti-SRCAP immunoaffinity chromatography to purify a native human S
76  and HBeAg, we used these Fabs in microscale immunoaffinity chromatography to purify HBeAg from indiv
77 urified from transformed Escherichia coli by immunoaffinity chromatography using a monoclonal antibod
78 bilized platelet membranes were subjected to immunoaffinity chromatography using an antibody raised a
79  for the proteolytic activity in the medium, immunoaffinity chromatography was performed.
80                                              Immunoaffinity chromatography was used to isolate the an
81                                           By immunoaffinity chromatography we enriched LeX glycoprote
82      Using a combination of ion exchange and immunoaffinity chromatography we have purified the gener
83 lf thymus pol delta preparations isolated by immunoaffinity chromatography were investigated.
84 ern blot analyses, immunohistochemistry, and immunoaffinity chromatography were used to detect and pu
85 compartments were seen following pulldown by immunoaffinity chromatography with Rab-specific antibodi
86 roteases inhibited by these serpins, we used immunoaffinity chromatography with serpin antibodies to
87 ication procedure (size, heparin, anion, and immunoaffinity chromatography): two heat shock proteins
88 h the receptor protein using both ligand and immunoaffinity chromatography, 2) TXA2 receptor activati
89       This was accomplished by using on-line immunoaffinity chromatography, a reverse-phase LC separa
90                 We used trypsin proteolysis, immunoaffinity chromatography, and tandem mass spectrome
91 e unlabeled apoB:1000 particles, isolated by immunoaffinity chromatography, contained 56 PL, 8 TAG, a
92 oisolated with PINCH from mammalian cells by immunoaffinity chromatography, indicating that PINCH and
93 usly pure mSR-BI-t1, prepared by single-step immunoaffinity chromatography, mediated high affinity HD
94                                        After immunoaffinity chromatography, the ORs are ~95% pure, an
95      Using a combination of conventional and immunoaffinity chromatography, we have successfully isol
96 n of endogenous levels of (FLAG)betabeta' by immunoaffinity chromatography, which was found to have 0
97 tion and 2) size exclusion-coupled anti-SOD1 immunoaffinity chromatography.
98 ast Saccharomyces cerevisiae and purified by immunoaffinity chromatography.
99 This was demonstrated by its isolation using immunoaffinity chromatography.
100  biochemically purified by sedimentation and immunoaffinity chromatography.
101 38 was associated with pol delta isolated by immunoaffinity chromatography.
102 bination of C(18) solid-phase extraction and immunoaffinity chromatography.
103 homogeneity in two steps by ion-exchange and immunoaffinity chromatography.
104 ns by conventional liquid chromatography and immunoaffinity chromatography.
105  by both standard biochemical techniques and immunoaffinity chromatography.
106 rom a pronase digest of Fap1 and purified by immunoaffinity chromatography.
107 orm have been purified from brain tubulin by immunoaffinity chromatography.
108 to detergent extraction and were purified by immunoaffinity chromatography.
109 orylated IGFBP-1 from normal human plasma by immunoaffinity chromatography.
110 rated in ripe fruit by gel filtration and by immunoaffinity chromatography.
111 e that had been purified and concentrated by immunoaffinity chromatography.
112 copy after 2-dimensional electrophoresis and immunoaffinity chromatography.
113 y traditional solvent extraction followed by immunoaffinity clean-up.
114                        The sensitivity using immunoaffinity cleanup was approximately 100-fold greate
115 treatment and centrifugation, followed by an immunoaffinity column (IAC) clean-up step before mass sp
116       Assay validation was performed against immunoaffinity column (IAC) tandem reversed-phase high p
117  liquid-liquid extraction, clean-up using an immunoaffinity column (IAC), and identification by rever
118 the types of antibodies that are used in the immunoaffinity column and by using an appropriate detect
119 n in bronchoalveolar lavage and an anti-SNIP immunoaffinity column binds a 70-kDa protein in U937 cel
120                                           By immunoaffinity column chromatography, we have purified t
121 trong cation-exchange chromatography and N60 immunoaffinity column chromatography.
122 fects of human Abs affinity-purified (AF) by immunoaffinity column chromotography on excitation-contr
123                                     Using an immunoaffinity column comprised of immobilized monoclona
124 munoadsorption (EIA) of anti-Gal Ab using an immunoaffinity column of a Gal type 6 oligosaccharide de
125 ter two-dimensional gel electrophoresis, and immunoaffinity column purification, N-terminal amino-aci
126 lso detected in the proteins eluted from the immunoaffinity column using serpin-6 antibody.
127              The nonretained peaks from this immunoaffinity column were passed through a series inter
128                After purification through an immunoaffinity column, AFM1 is determined by HPLC-FLD.
129                                     Using an immunoaffinity column, bovine brain tubulin was fraction
130                                The developed immunoaffinity column/capillary electrophoresis microdev
131 S method against sample preparation using an immunoaffinity column; the recovery and specificity were
132    Ochratoxin A analyses were performed with immunoaffinity columns and detection by high performance
133 gel filtration and associated with RNAPII on immunoaffinity columns prepared with anti-CTD antibodies
134 C instrumentation after pre-separation using immunoaffinity columns that work through a mechanism of
135 native cleanup procedures (MultiSep and IAC--immunoaffinity columns) was performed, being the advanta
136 using millisecond-scale extractions on small immunoaffinity columns.
137 re co-purified with GAD by specific anti-GAD immunoaffinity columns.
138 anol/water (80:20; v/v) and cleaned up using immunoaffinity columns.
139 Golgi membranes isolated from human liver by immunoaffinity contained native ARD1.
140  observation, we have developed a CD45-based immunoaffinity depletion method for removing CD45-contai
141                                        After immunoaffinity depletion of the most abundant serum prot
142 y, efficiencies of protein purification with immunoaffinity depletion were determined.
143 ll reproducibility of the process, including immunoaffinity depletion, is high, with a process replic
144 ity was achieved by applying front-end IgY14 immunoaffinity depletion.
145 me of sensitive and resistant cells using an immunoaffinity-enriched mass spectrometry method.
146 erived tryptic peptide via high-flow peptide immunoaffinity enrichment and nanoflow LC-MS/MS.
147 inase ubiquitination using ubiquitin remnant immunoaffinity enrichment and quantitative mass spectrom
148                                              Immunoaffinity enrichment coupled with quantitative mass
149              Mass spectrometry combined with immunoaffinity enrichment detects protein microheterogen
150                                              Immunoaffinity enrichment of peptides coupled with analy
151 e methods to characterize the performance of immunoaffinity enrichment of peptides up to multiplex le
152 DAMTS-13 substrate (vWFh) was performed with immunoaffinity enrichment of the reaction substrate and
153   The assay combines magnetic bead-based NGF immunoaffinity enrichment using a non-neutralizing polyc
154        MALDImmunoassays-methods that combine immunoaffinity enrichment with matrix-assisted laser des
155 gh-resolution mass spectrometry coupled with immunoaffinity enrichment, we identified 47 lysine-acety
156 alytes and solutions to carry out integrated immunoaffinity extraction and electrophoretic separation
157                       A new method, based on immunoaffinity extraction coupled with liquid chromatogr
158                                              Immunoaffinity extraction integrated with matrix-assiste
159 nd by performing computer simulations of the immunoaffinity extraction of these drugs.
160                                By optimizing immunoaffinity extraction using monoclonal antibodies co
161 whole spot was dissolved prior to cleanup by immunoaffinity extraction, tryptic digest, and preconcen
162 agments were isolated from plasma samples by immunoaffinity extraction.
163                            The use of a dual immunoaffinity fluorescent (IAF) tag permitted this proc
164 mated using the VICAM AflaTest and OchraTest immunoaffinity fluorometric method in a total of 50 meat
165                           Application of the immunoaffinity fluorometric method is an accurate, safe
166                  The novel BoNT demonstrated immunoaffinity for anti-A monoclonal antibodies but did
167 s strain behaved as a typical BoNT/B, having immunoaffinity for anti-B monoclonal antibodies and clea
168 from the liver was measured with a sensitive immunoaffinity/gas chromatography/high-resolution mass s
169 is presented, which involves coextraction by immunoaffinity (IA) beads and codetermination by selecte
170 pectrometry (LC/MS/MS) typically utilizes an immunoaffinity (IA) enrichment step such as immunoprecip
171  assay was developed utilizing two different immunoaffinity (IA) reagents.
172 chromatography/mass spectrometry analysis of immunoaffinity isolates of hippocampal neurons, that RAR
173                  In the present study, GLT-1 immunoaffinity isolates were prepared from rat cortex us
174                                   Rab5-based immunoaffinity isolation of IL-1beta-stimulated early en
175 ontaining each protein could be separated by immunoaffinity isolation; lectin binding showed that the
176 ion of a pronase digestion step prior to the immunoaffinity LC-MS/MS allowed for measuring not only f
177              A highly specific and sensitive immunoaffinity LC-MS/MS assay for quantification of huma
178                                           An immunoaffinity LC-MS/MS assay has been developed to quan
179           This work provides precedence that immunoaffinity LC-MS/MS can effectively be used to measu
180 tadiene for 90 days, using a newly developed immunoaffinity liquid chromatography tandem mass spectro
181                                        Using immunoaffinity liquid chromatography-mass spectrometry,
182                                           An immunoaffinity liquid chromatography-tandem mass spectro
183                    This article describes an immunoaffinity liquid chromatography-tandem mass spectro
184                                           An immunoaffinity liquid chromatography-tandem mass spectro
185               We describe a novel, sensitive immunoaffinity liquid chromatography-tandem mass spectro
186                                     Using an immunoaffinity mass spectrometry approach, a whole famil
187                  Sera were adsorbed on a Gal immunoaffinity matrix, and tested for SLA haplotype spec
188                                     Using an immunoaffinity method, we purified an MDM2-associated pr
189 intestinal lipoproteins were separated by an immunoaffinity method.
190 of 180 ms between the sample and an anti-BSA immunoaffinity microcolumn and provided a signal within
191                                              Immunoaffinity monolith pretreatment columns have been c
192                                 Here, we use immunoaffinity phosphopeptide isolation coupled with mas
193       Finally, we combine this approach with immunoaffinity phosphotyrosine enrichment, enabling the
194 we demonstrate using a combination of online immunoaffinity-postconcentration-mass spectrometry in co
195 ic target for HSV-1 infection, and a protein immunoaffinity procedure, we enriched fully glycosylated
196                          These two different immunoaffinity procedures yielded very similar sets of p
197 , we used a discovery platform consisting of immunoaffinity profiling coupled to mass spectrometry th
198 tive phosphorylation of STAT5 and applied an immunoaffinity profiling strategy to identify tyrosine-p
199 can be recognized by specific antibodies for immunoaffinity purification (IAP) and subsequent identif
200 elles containing TrkB isolated from brain by immunoaffinity purification also contain dynein with IC-
201 eract with Kir2 channels, as demonstrated by immunoaffinity purification and affinity chromatography
202     Specificity of antibody was confirmed by immunoaffinity purification and immunoabsorption.
203                                              Immunoaffinity purification and mass spectrometry reveal
204                                        Using immunoaffinity purification and mass spectrometry we sho
205                                        Using immunoaffinity purification and mass spectroscopy, we id
206                                              Immunoaffinity purification and microsequencing indicate
207 loyed proteomic screening by phosphotyrosine immunoaffinity purification and tandem mass spectrometry
208 the A17 membrane protein was demonstrated by immunoaffinity purification and Western blot analysis.
209        Herein, we have developed and used an immunoaffinity purification assay to isolate endogenous
210                                        Using immunoaffinity purification followed by mass spectrometr
211 um freudenreichii subsp. shermanii and after immunoaffinity purification in extracts of cereal matric
212 pecific recognition of PEGylated species, an immunoaffinity purification method (IAP) using anti-PEG
213         One of these antibodies was used for immunoaffinity purification of a protein that was identi
214                      Furthermore, the simple immunoaffinity purification of ABCB6 to near homogeneity
215                                              Immunoaffinity purification of AtMC1-containing complexe
216 d the exomic sequences of eight tumors after immunoaffinity purification of cancer cells.
217 rategy that incorporates rapid and efficient immunoaffinity purification of Complex I followed by dif
218 tity of proteins analyzed by LC-MS following immunoaffinity purification of IsoLG-modified proteins.
219 -denaturing conditions has made possible the immunoaffinity purification of labile, multisubunit enzy
220      The key steps in this approach involved immunoaffinity purification of Myl3 from serum followed
221                                              Immunoaffinity purification of polyribosomes (polysomes)
222 dividual serpin-1 isoforms in plasma we used immunoaffinity purification of serpin-1 isoforms from M.
223            Cell lysis, DNA fragmentation and immunoaffinity purification of the desired protein will
224  we established that tcTPC allowed stringent immunoaffinity purification of the gamma-secretase compl
225 ed from the infected cells were subjected to immunoaffinity purification of the tagged proteins by ad
226                                              Immunoaffinity purification of this protein and microseq
227 at represent 3 Bcr-Abl fusion types by using immunoaffinity purification of tyrosine phosphopeptides
228 d signaling intermediates were identified by immunoaffinity purification of tyrosine-phosphorylated p
229 undertaken by two independent approaches: 1) immunoaffinity purification on a mAb raised to condition
230  of 8-oxo-dGuo observed were confirmed by an immunoaffinity purification stable isotope dilution ([(1
231                   Our microdevices couple an immunoaffinity purification step with rapid microchip el
232 ibody-induced hearing loss, we used antibody immunoaffinity purification to isolate the IESCA, which
233                                        In an immunoaffinity purification using anti-HDAC3, transcript
234                                        Using immunoaffinity purification we show that hMUS81 or hMMS4
235 cted human embryonal kidney (HEK) 293 cells, immunoaffinity purification, and mass spectrometry combi
236 d characterized by rate-zonal sedimentation, immunoaffinity purification, electron microscopy, and th
237                     Through a combination of immunoaffinity purification, immobilized metal affinity
238 n tested for immunofluorescence staining and immunoaffinity purification, leading to putative identif
239                                        Using immunoaffinity purification, we isolated ribosomal prote
240 RF-NH(2)) by mass spectrometry combined with immunoaffinity purification.
241 in to the DRM-H fragments is confirmed by co-immunoaffinity purification.
242                                  Analysis of immunoaffinity purified (ALA)284(GLU) and (SER)289(LEU)
243      To investigate its function further, we immunoaffinity purified a bestrophin complex from RPE ly
244 LA-A*11:01 harvested from infected cells was immunoaffinity purified and acid boiled to release heavy
245                          Western blotting of immunoaffinity purified calf thymus pol delta revealed t
246                                      PSA was immunoaffinity purified from 100 to 200 ml of serum from
247 ble complex containing MLL1 and MOF has been immunoaffinity purified from a human cell line that stab
248                           Proteins were also immunoaffinity purified from brain extracts using autoan
249    UDP-N-acetylglucosamine pyrophosphorylase immunoaffinity purified from encysting and non-encysting
250 tion and by PCR analyses of epithelial cells immunoaffinity purified from primary tumors.
251                  To test this hypothesis, we immunoaffinity purified PI4KIIalpha from isotope-labeled
252 d from six independent Mediator preparations immunoaffinity purified through their Nut2 (MED10), Med2
253            Slowly sedimenting nucleoids were immunoaffinity purified using antibodies to either of tw
254 eplication, was readily recovered along with immunoaffinity-purified 3A-FLAG.
255                             The receptor was immunoaffinity-purified and formed functional InsP3- and
256                                 Furthermore, immunoaffinity-purified anti-cardiolipin antibodies from
257 Da as assessed by Western analyses utilizing immunoaffinity-purified antibody.
258 cDNA corresponding to the core protein of an immunoaffinity-purified arabinogalactan protein (AGP) se
259 rone assay after immunoprecipitation or with immunoaffinity-purified argpyrimidine-alpha-crystallin i
260 total OCP sera, IgG fractions from OCP sera, immunoaffinity-purified autoantibodies from sera of pati
261 eptide observed after PKC phosphorylation of immunoaffinity-purified Cx43.
262 s of these properties and the sufficiency of immunoaffinity-purified epitope-tagged AtPCS1 polypeptid
263  associated with Gbeta5 in the brain, it was immunoaffinity-purified from a nonionic detergent extrac
264                       The target antigen was immunoaffinity-purified from skeletal muscle extracts an
265 referentially over preexisting GABA by using immunoaffinity-purified GABAergic SVs.
266 was used to analyze proteins associated with immunoaffinity-purified HDL from plasma obtained from 2
267                                              Immunoaffinity-purified hsBG from transfected COS-1 cell
268 es were exposed to various concentrations of immunoaffinity-purified leukotoxin and the cytotoxicity
269                           Electroelution- or immunoaffinity-purified MTB 19-kDa lipoprotein inhibited
270                            We show here that immunoaffinity-purified native PmpD exists as an oligome
271 dicate that OCP sera, OCP IgG fractions, and immunoaffinity-purified OCP autoantibodies react with th
272 h OCP sera, IgG fractions from OCP sera, and immunoaffinity-purified OCP autoantibodies.
273 m a keratinocyte expression library by using immunoaffinity-purified OCP autoantibody, encoded the cy
274 and IgG fractions from 10 patients with OCP; immunoaffinity-purified OCP autoantibody; antibodies to
275                      The OP patient sera and immunoaffinity-purified OP sera, rabbit antisera against
276 e sequence analysis of a tryptic digest from immunoaffinity-purified Pa showed 100% identity to human
277                                              Immunoaffinity-purified PS contained 1.4 +/- 0.6 Zn(2+)/
278                                    Employing immunoaffinity-purified Rho from affected RHO(T4R/T4R) d
279 from the brain and lung extracts, and in the immunoaffinity-purified sample, but not in the negative
280                                              Immunoaffinity-purified TLF1 has a specific activity 10-
281 rylated intermediate chains were enriched on immunoaffinity-purified Trk-containing organelles.
282        This method distinguishes itself from immunoaffinity resin-based approaches since it can be sc
283 ion, giving rise to materials referred to as immunoaffinity restricted access media (IA-RAM).
284 cells were purified from spleens by negative immunoaffinity selection followed by flow sorting.
285                This method demonstrates true immunoaffinity separation of structurally related compou
286    The method involved analyte enrichment by immunoaffinity separation using anti-rhEPO antibody link
287 mprised analyte extraction and enrichment by immunoaffinity separation with anti-rhEPO antibodies, du
288 as isolated using solid-phase extraction and immunoaffinity separation.
289      Liquid-solid extraction, clean-up using immunoaffinity solid phase extraction chromatography, an
290 roduced in culture by first incorporating an immunoaffinity step using monoclonal antibodies to purif
291                    Western blot analyses and immunoaffinity studies confirmed that this protein was b
292 time considerably exceeded that of classical immunoaffinity systems.
293 taking advantage of the rhodopsin C-terminal immunoaffinity tag common to all GPCR constructs.
294 enaturing detergent digitonin and a one-step immunoaffinity technique.
295  purified the putative ATPDase from liver by immunoaffinity techniques and obtained a heavily glycosy
296  by density gradient ultracentrifugation and immunoaffinity techniques specific to apolipoprotein B-1
297 boratory to use LC/MS/MS in conjunction with immunoaffinity techniques to evaluate candidate biomarke
298 has been approached by mass spectrometry and immunoaffinity techniques.
299 ted that the prepared insulin still kept its immunoaffinity to its antibody.
300 loped a novel workflow integrating DNA-based immunoaffinity with mass spectrometry to analytically va

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